Cholecystitis
Symptom Information:
Symptom ID: | HPO:0001082 | ||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the liver(HPO:0001392) Abnormality of the biliary system(HPO:0004297) Abnormality of the gallbladder(HPO:0005264) Abnormal gallbladder physiology(HPO:0012438) Cholecystitis(HPO:0001082) MedDRA: Hepatobiliary disorders(MedDRA:10019805) Gallbladder disorders(MedDRA:10017628) Cholecystitis and cholelithiasis(MedDRA:10008616) Cholecystitis(HPO:0001082) |
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Database Frequency: | 9 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
Glycogen storage disease due to aldolase A deficiency | (Orphanet:57) |
Hemolytic anemia due to diphosphoglycerate mutase deficiency | (Orphanet:714) |
Hemolytic anemia due to glucophosphate isomerase deficiency | (Orphanet:712) |
Hemolytic anemia due to red cell pyruvate kinase deficiency | (Orphanet:766) |
Low phospholipid associated cholelithiasis | (Orphanet:69663) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
Non-spherocytic hemolytic anemia due to hexokinase deficiency | (Orphanet:90031) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Triose phosphate-isomerase deficiency | (Orphanet:868) |